Canonical Allele Identifier: CA2395758554
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177038G= , CM000684.2:g.19177038G= GRCh38
NC_000022.10:g.19164551G= , CM000684.1:g.19164551G= GRCh37
NC_000022.9:g.17544551G= NCBI36
NG_033863.1:g.6826C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.526+82C= MANE Select ENSP00000215882.5:n.526+82C=
ENST00000215882.9:c.526+82C= ENSP00000215882.5:n.526+82C=
ENST00000451283.5:c.217+82C= ENSP00000401480.1:n.217+82C=
ENST00000461267.1:n.672+82C=
ENST00000470922.5:n.668+82C=
NM_001256534.1:c.547+82C= NP_001243463.1:n.547+82C=
NM_001287387.1:c.217+82C= NP_001274316.1:n.217+82C=
NM_005984.4:c.526+82C= NP_005975.1:n.526+82C=
NR_046298.2:n.577+82C=
NM_005984.5:c.526+82C= MANE Select NP_005975.1:n.526+82C=
NM_001256534.2:c.547+82C= NP_001243463.1:n.547+82C=
NM_001287387.2:c.217+82C= NP_001274316.1:n.217+82C=
NR_046298.3:n.450+82C=